4.7 Article

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

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JOURNAL OF ORGANIC CHEMISTRY
卷 73, 期 13, 页码 5155-5158

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AMER CHEMICAL SOC
DOI: 10.1021/jo800749t

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  1. NIGMS NIH HHS [R01 GM063723, R01 GM063723-06S1, GM63723] Funding Source: Medline

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An improved protocol for the construction of enantioenriched pyrrolidine, indoline, and piperidine rings using an organo-catalyzed, intramolecular heteroatom Michael addition is described. Application to the enantioselective synthesis of homoproline, homopipecolic acid, and pelletierine has been accomplished.

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